US11078298B2ActiveUtilityPatentIndex 80
Antibodies to ubiquitin C-terminal hydrolase L1 (UCH-L1) and glial fibrillary acidic protein (GFAP) and related methods
Est. expiryOct 28, 2036(~10.3 yrs left)· nominal 20-yr term from priority
A61P 43/00C07K 2317/92C07K 2317/21C07K 2317/52G01N 33/6896A61P 31/22A61P 21/04A61P 29/00A61P 39/02A61P 31/04C07K 2317/20A61P 25/28C07K 16/40G01N 33/53A61P 31/12A61P 17/02A61P 25/00A61B 6/032C07K 2317/34C07K 2317/76A61P 33/14A61P 31/20A61B 5/0042A61P 9/00A61P 31/14C07K 2317/565A61P 25/16C07K 16/18A61P 31/00A61B 6/501A61P 9/10A61B 5/055
80
PatentIndex Score
12
Cited by
125
References
2
Claims
Abstract
The invention provides anti-UCH-L1 antibodies and anti-GFAP antibodies and their use in vitro detection of UCH-L1 and GFAP, respectively, in a sample from an individual, such as an individual known or suspected of having a brain injury or damage, for example, neurological damage such as mild traumatic brain injury. Also provided are methods, systems and kits for diagnosing brain injury or damage, such as neurological damage, in an individual with the aforementioned antibodies as well as compositions comprising the anti-UCH-L1 antibodies and anti-GFAP antibodies.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1. An antibody or antigen-binding fragment thereof that specifically binds to a human ubiquitin c-terminal hydrolase L I (UCH-L 1), wherein the antibody or antigen-binding fragment comprises a heavy chain variable region and a light chain variable region, wherein:
the heavy chain variable region comprises: (i) a CDR-HL comprising the amino acid sequence of SEQ ID NO:1; (ii) a CDR-H2 comprising the amino acid sequence of SEQ ID NO:9; and (iii) a CDR-H3 comprising the amino acid sequence of SEQ ID NO:20; and
wherein the light chain variable region comprises: (i) a CDR-LI comprising the amino acid sequence of SEQ ID NO:28; (ii) a CDR-L2 comprising the amino acid sequence of SEQ ID NO:37; and (iii) a CDR-L3 comprising the amino acid sequence of SEQ ID NO:45.
2. A composition comprising the antibody or antigen-binding fragment of claim 1 .Cited by (0)
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